Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion description "[We dichotomized the whole cohort based on the presence or absence of N34S SPINK1 and L26V CTSB mutations and further subdivided them into TCP and FCPD patients and compared the distribution of TCF7L2 variants between them.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion evidence source_evidence_literature NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion SIO_000772 18706099 NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion wasDerivedFrom befree-20140225 NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_assertion wasGeneratedBy ECO_0000203 NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP214399.RAIm-VBlV2XAylFSil77vBkdF8gE7PRDfLgKa7O9N-LPU130_provenance.